NM_004977.3(KCNC3):c.2093G>A (p.Arg698His) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 17, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001644605.1
Allele description [Variation Report for NM_004977.3(KCNC3):c.2093G>A (p.Arg698His)]
NM_004977.3(KCNC3):c.2093G>A (p.Arg698His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024